IGVFFI2319YGLG

preview

validated

This object is in preview status. Metadata is subject to change until this object is released.

File Set

IGVFDS0170TMBA(gRNA sequencing for CRISPR interference Perturb-seq integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci)

Summary

R2 reads from sequencing run 1

File Format

fastq

Content Type

reads

Aliases

gary-hon:LW422B_6_R2

md5sum

063ba3cf4bc6e8dc01dc35950fdc34d9

Content MD5sum

14bf760afbf32d5dd236263363592ce7

File Size

9.2 GB

Submitted File Name

/project/GCRB/Hon_lab/shared/data/sequencing_data/2024/2024-05-01-Novogene-NovaSeq.Hon19_20/sgRNA//LW422B_S2_L006_R2_001.fastq.gz

Checkfiles Version

Legacy version of checkfiles

Sequencing Details

Sequencing Platform

Illumina NovaSeq X Plus

Sequencing Run

Flowcell ID

227C7WLT4

Lane

Sequencing Kit

NovaSeq X Series 25B Reagent Kit

Illumina Read Type

Average Read Length

151

Read Count

167643252

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM8986CPUS

InVitroSystem

H9 differentiated cell specimen induced to cardiac muscle cell for 12 days (cellular sub pool: subpool_LW422), female, Homo sapiens modified with CRISPRi Sp-dCas9, transduced (lentivirus) with a guide library